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NEISSERIA SP - ANVISA Registration 80537410143

Access comprehensive regulatory information for NEISSERIA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80537410143 and manufactured by manufacturer not specified. The registration is held by CELER BIOTECNOLOGIA S/A with validity until Jun 30, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including QIAGEN, BECTON, DICKINSON AND COMPANY, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80537410143
2 Related Devices
Registration Details
ANVISA Registration Number: 80537410143
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Related Devices (2)

GONORREIA TESTE RÁPIDO CELER
Risk Class IV

Registration Details

80537410143

25351016522202531

04846613000103

Company Information

Dates and Status

Jun 30, 2025

30/06/2035

09/18/2025 19:00:01

GONORREIA TESTE RÁPIDO CELER
Risk Class IV

Registration Details

80537410143

25351016522202531

04846613000103

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 30, 2025

30/06/2035

09/18/2025 19:00:01